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OREGON SCINTIFIC

K131245 Class II Traditional
Decision Date
2014-01-17
Sponsor / Applicant
Idt Technology Limited

Technical Specification

510(k) Submission ID K131245
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2014-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OREGON SCINTIFIC received FDA 510(k) clearance under submission number K131245, sponsored by Idt Technology Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.